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JP2008536125A5
JP2008536125A5 JP2008505549A JP2008505549A JP2008536125A5 JP 2008536125 A5 JP2008536125 A5 JP 2008536125A5 JP 2008505549 A JP2008505549 A JP 2008505549A JP 2008505549 A JP2008505549 A JP 2008505549A JP 2008536125 A5 JP2008536125 A5 JP 2008536125A5
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analyte
internal reference
reference compound
potential
control solution
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Claims (10)

コントロール溶液およびサンプル中の分析目的物の量を測定する電気化学的センサの操作中に、コントロール溶液をサンプルから区別する方法であって:
(a) コントロール溶液に対して、分析目的物の酸化を測定するのに必要な電位よりも高い電位で電気化学的に酸化されるように構成される内部基準化合物を添加する工程;
(b) 内部基準化合物および所定量の分析目的物を含むコントロール溶液を、作用電極およびカウンタ電極、および試薬を有する電気化学的センサへ導入する工程;
(c) 電気化学的センサに対して、内部基準化合物および分析目的物を酸化するのに十分な電位を少なくとも一回印加して、結果的に生じる電流を測定する工程;
(d) 電気化学的センサに(c)の電位よりも低く、分析目的物の酸化を測定するのに十分なものであるが、内部基準化合物を酸化するには不十分である電位を少なくとも一回印加し、結果的に生じる電流を測定する工程;
(e) DI = ihigh volt / i low volt〔式中、i high voltは(c)で測定された電流値であり、i low voltは(d)で測定された電流値である〕として定義されたディファレンシャル・インデックス(DI)を計算する工程;
(f) 内部基準化合物を所定量の分析目的物と区別するように(e)でのディファレンシャル・インデックスが1より十分に大きい場合、コントロール溶液が存在すると決定する工程;および
(g) (e)でのディファレンシャル・インデックスが約1である場合にサンプルが存在すると決定する工程;
を含む前記方法。
A method of distinguishing a control solution from a sample during operation of an electrochemical sensor that measures the amount of analyte in the control solution and sample:
(A) adding to the control solution an internal reference compound configured to be electrochemically oxidized at a potential higher than that required to measure the oxidation of the analyte;
(B) introducing a control solution containing an internal reference compound and a predetermined amount of an analyte into an electrochemical sensor having a working electrode and a counter electrode, and a reagent;
(C) applying to the electrochemical sensor at least one potential sufficient to oxidize the internal reference compound and the analyte and measuring the resulting current;
(D) At least one potential that is lower than the potential of (c) in the electrochemical sensor and sufficient to measure the oxidation of the analyte of interest, but insufficient to oxidize the internal reference compound. Applying multiple times and measuring the resulting current;
(E) DI = i high volt / i low volt where i high volt is the current value measured in (c) and i low volt is the current value measured in (d) Calculating a differentiated differential index (DI);
(F) determining that a control solution is present if the differential index in (e) is sufficiently greater than 1 to distinguish the internal reference compound from a predetermined amount of analyte; and (g) (e) Determining that a sample is present if the differential index at is about 1;
Including said method.
(f)で決定されたディファレンシャル・インデックスが1.5またはそれより高い、請求項1の方法。   The method of claim 1, wherein the differential index determined in (f) is 1.5 or higher. コントロール溶液中に存在する分析目的物の量に比例した量で内部基準化合物が添加される、請求項1の方法。   The method of claim 1, wherein the internal reference compound is added in an amount proportional to the amount of analyte present in the control solution. 分析目的物を酸化するのに十分な第一の電位を第一の所定時間印加し、引き続いて分析目的物を酸化するには不十分な第一の電位より低い第二の電位を第二の所定時間印加し、そしてその後分析目的物を酸化するのに十分な第二の電位より高い第三の電位を第三の所定時間印加することによって、分析目的物が測定される、請求項1の方法。   A first potential sufficient to oxidize the analyte is applied for a first predetermined time, followed by a second potential that is less than the first potential insufficient to oxidize the analyte. 2. The analyte of interest is measured by applying a predetermined time and then applying a third potential higher than a second potential sufficient to oxidize the analyte for a third predetermined time. Method. 分析目的物がグルコースであり、サンプルが全血である、請求項1の方法。   The method of claim 1, wherein the analyte is glucose and the sample is whole blood. 内部基準化合物が、酸化可能な有機金属化合物、配位化合物または有機アミン化合物である、請求項1の方法。   The method of claim 1, wherein the internal reference compound is an oxidizable organometallic compound, a coordination compound, or an organic amine compound. 内部基準化合物が、3-(N-モルホリノ)プロパンスルホン酸、N-(2-ヒドロキシエチル)ピペラジン-N1-(2-エタンスルホン酸)、2-[2-ヒドロキシ-1,1-bis(ヒドロキシメチル)エチルアミノ]エタンスルホン酸、2-モルホリノエタンスルホン酸、およびBis(2-ヒドロキシエチル)アミノ-tris(ヒドロキシメチル)メタン[Bis-Tris]、4-アミノベンゾニトリル、4-アミノ安息香酸、または4-ヨードアニリンである有機アミン化合物である、請求項6の方法。 Internal reference compounds are 3- (N-morpholino) propanesulfonic acid, N- (2-hydroxyethyl) piperazine-N 1- (2-ethanesulfonic acid), 2- [2-hydroxy-1,1-bis ( Hydroxymethyl) ethylamino] ethanesulfonic acid, 2-morpholinoethanesulfonic acid, and Bis (2-hydroxyethyl) amino-tris (hydroxymethyl) methane [Bis-Tris], 4-aminobenzonitrile, 4-aminobenzoic acid Or an organic amine compound that is 4-iodoaniline. 内部基準化合物が、フェロシアン化カリウムである配位化合物である、請求項6の方法。   7. The method of claim 6, wherein the internal reference compound is a coordination compound that is potassium ferrocyanide. (a) 所定量の分析目的物;および
(b) 分析目的物を酸化するために必要とされる電位よりも高い電位で酸化されるように構成され、内部基準化合物の存在を検出可能になるように所定量の内部基準化合物は所定量の分析目的物と比例する、所定量の内部基準化合物;
を含む、サンプル中の分析目的物の量を測定するための電気化学的システムの試験を行う際に用いられるコントロール溶液。
(A) a predetermined amount of the analyte of interest; and (b) configured to be oxidized at a potential higher than that required to oxidize the analyte of interest so that the presence of an internal reference compound can be detected. The predetermined amount of the internal reference compound is proportional to the predetermined amount of the analyte, the predetermined amount of the internal reference compound;
A control solution used in testing an electrochemical system for measuring the amount of an analyte in a sample.
分析目的物の量を測定する電気化学的センサの操作中に、コントロール溶液をサンプルから区別する方法であって:
内部基準化合物であって分析目的物の酸化を測定するために必要とされる電位よりも高い電位を有しそしてバッファとは異なるもの、バッファおよび所定量の分析目的物を含むコントロール溶液を用意する工程;
作用電極およびカウンタ電極を有する電気化学的センサを用意する工程;
コントロール溶液を電気化学的センサへ導入する工程;
内部基準化合物および分析目的物を酸化するのに十分な電位を電気化学的センサに対して印加し、そして生じる電流を測定する工程;
分析目的物を酸化するには十分であるが内部基準化合物を酸化するには十分ではないより低い電位を電気化学的センサに対して印加し、そして生じる電流を測定する工程;そして
測定された電流に基づいて、コントロール溶液またはサンプルが存在するかどうかを決定する工程;
を含む前記方法。
A method for distinguishing a control solution from a sample during operation of an electrochemical sensor for measuring the amount of an analyte of interest:
Prepare a control solution that is an internal reference compound that has a potential higher than that required to measure the oxidation of the analyte and is different from the buffer, including a buffer and a predetermined amount of the analyte. Process;
Providing an electrochemical sensor having a working electrode and a counter electrode;
Introducing the control solution into the electrochemical sensor;
Applying a sufficient potential to the electrochemical sensor to oxidize the internal reference compound and the analyte and measuring the resulting current;
Applying a lower potential to the electrochemical sensor sufficient to oxidize the analyte of interest but not sufficient to oxidize the internal reference compound and measuring the resulting current; and measured current Determining whether a control solution or sample is present based on:
Including said method.
JP2008505549A 2005-04-08 2006-04-07 Oxidizable species as an internal reference in control solutions for biosensors Active JP5009897B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US66972905P 2005-04-08 2005-04-08
US60/669,729 2005-04-08
PCT/US2006/012940 WO2006110504A1 (en) 2005-04-08 2006-04-07 Oxidizable species as an internal reference in control solutions for biosensors

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JP2008536125A JP2008536125A (en) 2008-09-04
JP2008536125A5 true JP2008536125A5 (en) 2009-05-14
JP5009897B2 JP5009897B2 (en) 2012-08-22

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US (4) US8002965B2 (en)
EP (2) EP1869203B1 (en)
JP (1) JP5009897B2 (en)
CN (3) CN102778487B (en)
BR (1) BRPI0609633B1 (en)
CA (1) CA2603542C (en)
DK (1) DK2267150T3 (en)
ES (1) ES2552083T3 (en)
HK (1) HK1205258A1 (en)
MX (1) MX2007012373A (en)
NO (1) NO20075709L (en)
PL (1) PL2267150T3 (en)
RU (1) RU2453843C2 (en)
TW (1) TW200641352A (en)
WO (1) WO2006110504A1 (en)

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